| Literature DB >> 33717201 |
Xiao Yuan1, Jinxi Wang2, Yixuan Huang3, Dangang Shangguan4, Peng Zhang3.
Abstract
Immune infiltrates in the tumor microenvironment (TME) of breast cancer (BRCA) have been shown to play a critical role in tumorigenesis, progression, invasion, and therapy resistance, and thereby will affect the clinical outcomes of BRCA patients. However, a wide range of intratumoral heterogeneity shaped by the tumor cells and immune cells in the surrounding microenvironment is a major obstacle in understanding and treating BRCA. Recent progress in single-cell technologies such as single-cell RNA sequencing (scRNA-seq), mass cytometry, and digital spatial profiling has enabled the detailed characterization of intratumoral immune cells and vastly improved our understanding of less-defined cell subsets in the tumor immune environment. By measuring transcriptomes or proteomics at the single-cell level, it provides an unprecedented view of the cellular architecture consist of phenotypical and functional diversities of tumor-infiltrating immune cells. In this review, we focus on landmark studies of single-cell profiling of immunological heterogeneity in the TME, and discuss its clinical applications, translational outlook, and limitations in breast cancer studies.Entities:
Keywords: breast cancer; immune cell; single cell mass cytometry; single-cell sequencing; tumor microenviroment
Year: 2021 PMID: 33717201 PMCID: PMC7947360 DOI: 10.3389/fimmu.2021.643692
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561